Quantification of vascular endothelial growth factor-C and its receptor-3 messenger RNA with real-time quantitative polymerase chain reaction as a predictor of lymph node metastasis in human colorectal cancer

被引:75
作者
Kawakami, M
Furuhata, T
Kimura, Y
Yamaguchi, K
Hata, F
Sasaki, K
Hirata, K
机构
[1] Sapporo Med Univ, Dept Surg 1, Chuo Ku, Sapporo, Hokkaido 0608543, Japan
[2] Doto Hosp, Dept Surg, Sapporo, Hokkaido, Japan
关键词
D O I
10.1067/msy.2003.45
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background. This study was undertaken to determine whether vascular endothelial growth factor-C (VEGF-C) and the expression of its receptor VEGF receptor-3 (VEGFR-3) are correlated with lymph node metastasis in human colorectal cancer and whether their expression levels might be used to predict lymph node metastasis. Methods. Fifty-three surgical specimens of colorectal cancer with (n = 24) or without (n = 29) lymph node metastasis were studied. The messenger RNA (mRNA) expression of VEGF-C and VEGER-3 was quantified with a new method for kinetic quantitative polymerase chain reaction (PCR), real-time quantitative (RTQ) reverse transcriptase-PCR. In addition, their protein expressions were assessed immunohistochemically. Results. The VEGF-C mRNA level in primary tumors correlated with VEGF-C protein expression, lymph node metastasis, and lymphatic invasion. Sixteen of 24 patients with lymph node metastasis showed VEGF-C mRNA overexpression. Morphologically, VEGF-C protein expression in primary tumors showed a statistically significant relationship with lymph node metastasis and lymphatic invasion. Conclusion. Real-time quantitative reverse transcriptase-PCR is a sensitive method for detection and quantification of VEGF-C and VEGER-3 mRNA expression. Furthermore, the expression levels of VEGF-C mRNA and protein in colorectal cancer are correlated with lymph node metastasis and lymphatic invasion.
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页码:300 / 308
页数:9
相关论文
共 26 条
[1]   Vascular endothelial growth factor-C (VEGF-C) expression in human colorectal cancer tissues [J].
Akagi, K ;
Ikeda, Y ;
Miyazaki, M ;
Abe, T ;
Kinoshita, J ;
Maehara, Y ;
Sugimachi, K .
BRITISH JOURNAL OF CANCER, 2000, 83 (07) :887-891
[2]  
Bièche I, 1998, INT J CANCER, V78, P661, DOI 10.1002/(SICI)1097-0215(19981123)78:5<661::AID-IJC22>3.3.CO
[3]  
2-9
[4]   Expression of angiogenesis stimulators and inhibitors in human thyroid tumors and correlation with clinical pathological features [J].
Bunone, G ;
Vigneri, P ;
Mariani, L ;
Butó, S ;
Collini, P ;
Pilotti, S ;
Pierotti, MA ;
Bongarzone, I .
AMERICAN JOURNAL OF PATHOLOGY, 1999, 155 (06) :1967-1976
[5]   Vascular endothelial growth factor-C gene expression in papillary and follicular thyroid carcinomas [J].
Fellmer, PT ;
Sato, K ;
Tanaka, R ;
Okamoto, T ;
Kato, Y ;
Kobayashi, M ;
Shibuya, M ;
Obara, T .
SURGERY, 1999, 126 (06) :1056-1061
[6]   Real-time quantitative RT-PCR after laser-assisted cell picking [J].
Fink, L ;
Seeger, W ;
Ermert, L ;
Hänze, J ;
Stahl, U ;
Grimminger, F ;
Kummer, W ;
Bohle, RM .
NATURE MEDICINE, 1998, 4 (11) :1329-1333
[7]   Seminars in medicine of the Beth Israel Hospital, Boston - Clinical applications of research on angiogenesis [J].
Folkman, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (26) :1757-1763
[8]  
Gerard CJ, 1998, CANCER RES, V58, P3957
[9]   Real time quantitative PCR [J].
Heid, CA ;
Stevens, J ;
Livak, KJ ;
Williams, PM .
GENOME RESEARCH, 1996, 6 (10) :986-994
[10]   Hyperplasia of lymphatic vessels in VEGF-C transgenic mice [J].
Jeltsch, M ;
Kaipainen, A ;
Joukov, V ;
Meng, XJ ;
Lakso, M ;
Rauvala, H ;
Swartz, M ;
Fukumura, D ;
Jain, RK ;
Alitalo, K .
SCIENCE, 1997, 276 (5317) :1423-1425